Reaktion #3985

ord-abd517df60204610939cf68a6c24b096

Reaktionsgleichung

NC1CCN(Cc2ccc3ccccc3c2)CC1
4-Amino-1-(naphth-2-ylmethyl)piperidine
O=C(N=C=S)c1ccccc1
benzoylisothiocyanate
O=C(NC(=S)NC1CCN(Cc2ccc3ccccc3c2)CC1)c1ccccc1
1-Benzoyl-3-[1-(naphth-2-ylmethyl)piperid-4-yl]thiourea

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was evaporated
  2. 2
    workup.DISSOLUTIONthe gum dissolved in isopropyl alcohol
  3. 3
    SonstigeThe solvent was evaporated
  4. 4
    workup.DISSOLUTIONthe residue dissolved in ethyl acetate
  5. 5
    SonstigeThe title compound crystallised
  6. 6
    Filtrationwas filtered
  7. 7
    Trocknendried as the monohydrochloride quarterhydrate salt, m.p. 212°-214° C.

Vorschrift

4-Amino-1-(naphth-2-ylmethyl)piperidine (1.0 g, 0.0042 m) and benzoylisothiocyanate (0.69 g, 0.0042 m) in toluene (120 cm3) was stirred at room temperature for 6 hours. The solvent was evaporated and the gum dissolved in isopropyl alcohol and acidified with ethanolic HCl. The solvent was evaporated and the residue dissolved in ethyl acetate. The title compound crystallised and was filtered and dried as the monohydrochloride quarterhydrate salt, m.p. 212°-214° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04722930uspto-grants-1988_02